DE LA CRUZ TINCTURE OF IODINE- iodine and sodium iodide and alcohol liquid

De La Cruz Tincture of Iodine by

Drug Labeling and Warnings

De La Cruz Tincture of Iodine by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Iodine 2%, Sodium Iodide 2.4%

Purpose

First aid antiseptic

Uses

First aid antiseptic to help prevent infection in minor:

• cuts
• scrapes
• burns

Warnings

For external use only

Flammable. Keep away from sparks, heat and fire.

Consult a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not use in or near the eyes. If eye contact occurs, flush with large amounts of water while lifting upper and lower lids.
• do not apply over large areas of the body

Stop use and consult a doctor if

• the condition persists or gets worse. Do not use this product longer than 1 week unless directed by a doctor.

Keep out of reach of children.

If swallowed, give milk then give a starch solution made by mixing 2 tablespoons of corn starch or flour to a pint of water. Contact a Poison Control Center immediately.

Directions

• clean the affected area
• apply a small amount of this product to the area 1 to 3 times daily
• may be covered with a sterile bandage. If bandaged, let dry first.

Other information

• will stain skin and clothing
• store at room temperature

Inactive ingredients

alcohol, purified water

Questions

1-800-858-3889

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Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label

De La Cruz®

Tincture
of Iodine

USP 2% Alcohol 47%

First Aid Antiseptic

TRUSTED
QUALITY

For External Use Only

POISON / DANGER

1 FL OZ
(30 mL)

INGREDIENTS AND APPEARANCE

DE LA CRUZ TINCTURE OF IODINE 
iodine and sodium iodide and alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1528
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	20 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1528-7	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/27/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/1979

Labeler - DLC Laboratories, Inc. (093351930)

Registrant - Humco Holding Group, Inc (825672884)